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The morphology of xenotransplanted human breast carcinoma MX-1 growing in nude mice. A light and transmission electron microscopic study.

Abstract
The present investigation is concerned with the morphological features of the human breast carcinoma MX-1, transplanted subcutaneously into nude mice. Three weeks after transplantation the tumor tissue is clearly distinct from the dermis. Solid tumor cell groups are separated incompletely by thin connective tissue septa, giving rise to a lobular appearance. The tumor cells are characterized by very irregularly formed nuclei with three or more nucleoli. The cytoplasm of these cells displays some lysosomes, the cisternae of the rough endoplasmic reticulum, mitochondria and a variable number of ribosomes. The Golgi fields are frequently observed, particularly near the nucleus. The cells are connected to each other by desmosomes, which also persist during mitotic activity. Ductular formations can occasionally be seen. The ultrastructure of the blood vessels discloses the morphological features necessary for the regulation of blood flow. Capillaries present a sinusoidal aspect with distended and narrow lumina. Interruptions of the endothelial wall, however, were not observed. This morphological appearance was found in all the MX-1 tumors investigated, reflecting the stable growth of this tumor cell line in nude mice.
AuthorsA S Mendoza, M Mentzel, M Krüger, H J Krammer, G Wiedemann, T Wagner, C Weiss, W Kühnel
JournalAnnals of anatomy = Anatomischer Anzeiger : official organ of the Anatomische Gesellschaft (Ann Anat) Vol. 177 Issue 1 Pg. 3-10 (Jan 1995) ISSN: 0940-9602 [Print] GERMANY
PMID7872494 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Topics
  • Animals
  • Breast Neoplasms (blood supply, pathology, ultrastructure)
  • Capillaries (pathology, ultrastructure)
  • Cell Line
  • Female
  • Humans
  • Mice
  • Mice, Nude
  • Microscopy, Electron
  • Nerve Fibers (pathology, ultrastructure)
  • Transplantation, Heterologous
  • Tumor Cells, Cultured

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